Data / Medical devices / China / Suzhou Pipi Medical Products Co.,ltd
Suzhou Pipi Medical Products Co.,ltd: FDA-registered device maker in Suzhou Jiangsu, China, 1 510(k) clearance
Suzhou Pipi Medical Products Co.,ltd is registered with the FDA (registration 3009308092) in Suzhou Jiangsu, China. It lists 48 device types. The FDA files 1 510(k) clearance under its listings, the newest dated January 7, 2010. Registered through 2027. FDA data exported November 2, 2026.
SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.
- FDA registration number
- 3009308092
- Address
- No.139 WeiHe Road, #2 Building, 7th Floor SuZhou Industries Park, Suzhou Jiangsu, China, 215122
- Owner or operator
- SuZhou PiPi Medical Products Co., Ltd (10037836)
- Roles
- Contract manufacturer, Exporter to the US, Manufacturer, Repackager or relabeler
- First device listed
- August 24, 2011
- Registered through
- 2027
- Brand names listed
- Baby Footprinter, Bandage, Bath sponge, Bib, Bra Pads; Breast Pads; Disposable Bra Pads; Disposable Breast Pads; Disposable Nursing Pads; Nursing Pads, Bulb Syringe, CORD CLAMP CLIPPERS, Diabetic foot test monofilament and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|
| Absorber, Saliva, Paper | KHR | 1 | Exporter to the US | accessdata.fda.gov |
| Accessories, Catheter | KGZ | 1 | Exporter to the US | accessdata.fda.gov |
| Accessory, Surgical Apparel | LYU | 1 | Manufacturer | accessdata.fda.gov |
| Adaptor, Dressing | ILD | 1 | Exporter to the US | accessdata.fda.gov |
| Adaptor, Hygiene | ILS | 1 | Manufacturer | accessdata.fda.gov |
| Aid, Transfer | IKX | 1 | Exporter to the US | accessdata.fda.gov |
| Armrest, Wheelchair | IML | 1 | Exporter to the US | accessdata.fda.gov |
| Bag, Ice | KYR | 1 | Exporter to the US | accessdata.fda.gov |
| Bandage, Elastic | FQM | 1 | Contract manufacturer, Manufacturer | accessdata.fda.gov |
| Bedding, Disposable, Medical | KME | 1 | Exporter to the US | accessdata.fda.gov |
| Bottle, Hot/Cold Water | FPF | 1 | Contract manufacturer, Manufacturer | accessdata.fda.gov |
| Components, Exercise | IOD | 1 | Contract manufacturer | accessdata.fda.gov |
| Container, Specimen Mailer And Storage, Non-Sterile | NNK | 1 | Manufacturer | accessdata.fda.gov |
| Container, Specimen, Sterile | FMH | 1 | Exporter to the US | accessdata.fda.gov |
| Continuous Measurement Thermometer | FLL | 2 | Exporter to the US | accessdata.fda.gov |
| Depressor, Tongue, Non-Surgical | FMA | 1 | Exporter to the US | accessdata.fda.gov |
| Device, Incontinence, Urosheath Type, Sterile | EXJ | 1 | Exporter to the US | accessdata.fda.gov |
| Device, Occlusion, Umbilical | FOD | 1 | Exporter to the US | accessdata.fda.gov |
| Dispenser, Liquid Medication | KYX | 1 | Exporter to the US | accessdata.fda.gov |
| Dispenser, Solid Medication | NXB | 1 | Exporter to the US | accessdata.fda.gov |
| Esthesiometer | GXB | 1 | Repackager or relabeler | accessdata.fda.gov |
| First Aid Kit Without Drug | OHO | 1 | Exporter to the US | accessdata.fda.gov |
| Forceps | HTD | 1 | Exporter to the US | accessdata.fda.gov |
| Gauze / Sponge,Nonresorbable For External Use | NAB | 1 | Exporter to the US | accessdata.fda.gov |
| Light, Examination, Medical, Battery Powered | KYT | 1 | Exporter to the US, Manufacturer | accessdata.fda.gov |
| Marker, Skin | FZZ | 1 | Exporter to the US | accessdata.fda.gov |
| Mask, Scavenging | KHA | 1 | Exporter to the US | accessdata.fda.gov |
| Non-Surgical Gown | OEA | 1 | Exporter to the US | accessdata.fda.gov |
| Nursing Pad, Polyurethane Pad With Starch Copolymer, Glycerin, And Surfactant (F-68) | NTX | 1 | Exporter to the US | accessdata.fda.gov |
| Pill Crusher/Cutter | OHY | 1 | Manufacturer | accessdata.fda.gov |
| Protector, Skin Pressure | FMP | 1 | Manufacturer | accessdata.fda.gov |
| Razor, Surgical | LWK | 1 | Exporter to the US | accessdata.fda.gov |
| Ring Cutter | FNS | 1 | Exporter to the US, Manufacturer | accessdata.fda.gov |
| Scissors, General, Surgical | LRW | 1 | Exporter to the US | accessdata.fda.gov |
| Scissors, Umbilical | HDJ | 1 | Exporter to the US | accessdata.fda.gov |
| Scraper, Tongue | LCN | 1 | Exporter to the US | accessdata.fda.gov |
| Shield, Eye, Ophthalmic (Including Sunlamp Protective Eyewear And Post-Mydriatic Eyewear) | HOY | 1 | Contract manufacturer, Exporter to the US | accessdata.fda.gov |
| Shoe And Shoe Cover, Conductive | BWP | 1 | Exporter to the US | accessdata.fda.gov |
| Shoe, Cast | IPG | 1 | Exporter to the US, Manufacturer | accessdata.fda.gov |
| Spectacle, Magnifying | HOI | 1 | Exporter to the US | accessdata.fda.gov |
| Speculum, Vaginal, Nonmetal | HIB | 2 | Exporter to the US | accessdata.fda.gov |
| Strip, Temperature, Forehead, Liquid Crystal | KPD | 2 | Exporter to the US | accessdata.fda.gov |
| Syringe, Irrigating (Non Dental) | KYZ | 1 | Manufacturer | accessdata.fda.gov |
| Tape And Bandage, Adhesive | KGX | 1 | Exporter to the US | accessdata.fda.gov |
| Tape, Measuring, Rulers And Calipers | FTY | 1 | Manufacturer | accessdata.fda.gov |
| Tips And Pads, Cane, Crutch And Walker | INP | 1 | Manufacturer | accessdata.fda.gov |
| Toothbrush, Manual | EFW | 1 | Exporter to the US, Manufacturer | accessdata.fda.gov |
| Tourniquet, Nonpneumatic | GAX | 1 | Exporter to the US | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|
| January 7, 2010 | K092447 | DIGITAL THERMOMETER (WITH DISPOSABLE THERMOMETER COVER), DT SERIES | FLL | Substantially Equivalent | Hangzhou Hua'An Medical & Health Instruments Co., | accessdata.fda.gov |
Compare with other makers
Updated January 7, 2010. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.